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Paper Details

A mutation creating an out-of-frame alternative translation initiation site in the GRHPR 5'UTR causing primary hyperoxaluria type II.
Clin Genet
7
2015
-of-frame translational start site, 5'untranslated region, 694delC, GRHPR, GRHPR 5'UTR, GRHPR gene, GRHPR proximal promoter, Gln, Gln232Argfs, Primary hyperoxaluria type II, UTR, c, canonical translation initiation site, canonical translational start site, luciferase reporter, man, out-of-frame alternative translation initiation site, primary hyperoxaluria type II, recessive genetic disorder, single-nucleotide deletion, variant start site
Author NameAffiliation
Yi FuOregon Health & Science University and the Portland VA Medical Center
Yi FuOregon Health & Science University and the Portland VA Medical Center
Robert RopeOregon Health & Science University and the Portland VA Medical Center
David M CohenOregon Health & Science University and the Portland VA Medical Center
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